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<h3>Job Description</h3>
Job Description
Ascendis Pharma is a dynamic, fast-growing global biopharmaceutical company with locations in Denmark, Europe, and the United States. Today, we're advancing programs in Endocrinology Rare Disease and Oncology.
Here at Ascendis, we pride ourselves on exceptional science, visionary leadership, and skilled and passionate colleagues.
Guided by our core values of Patients, Science, and Passion, we use our TransCon® drug development platform to fulfill our mission of developing new and potentially best-in-class therapies to address unmet medical needs.
Our culture fosters a place where skilled, adaptable, and highly resourceful professionals can truly make their mark. We offer a dynamic workplace for employees to grow and develop their skills.
The Senior Clinical Scientist is involved in the design, monitoring, and data analysis of the Company’s late-phase clinical trials studying growth hormone, parathyroid hormone, and/or C-type natriuretic peptide therapies. As such, the Senior Clinical Scientist is an important and visible member of the Clinical Development team. The Senior Clinical Scientist position is based in the United States ideally the Scientist will work hybrid from our Palo Alto, CA office but we may consider a remote arrangement for the right candidate.
Key Responsibilities
<ul>
<li>For clinical trials: design, provide oversight, and support site and subject retention </li>
<li>Ensure successful completion of documents (including clinical trial protocols, investigator brochures, monitoring plans, site training materials, clinical study reports, health authority responses, standard operating procedures, etc.) with cross-functional team members</li>
<li>Participate on study teams and cross-functional teams as appropriate, and as delegated by the Vice President, Clinical Development</li>
<li>Ensure consistent use of language and criteria across multiple endocrine projects </li>
<li>Ensure study integrity, and track accumulating safety and efficacy data</li>
<li>Anticipate obstacles within a clinical trial, and implement solutions</li>
<li>Analyze, evaluate, and support accurate interpretation and reporting of clinical data</li>
<li>Contribute to drafting and reviewing clinical documents, manuscripts, presentations, and regulatory submissions </li>
<li>Maintain up-to-date knowledge of relevant science, medical information, good clinical practices, and regulatory guidance</li>
<li>Collaborate with—and serve as a clinical research resource for—cross-functional colleagues to optimize product development</li>
<li>Cultivate relationships with investigative sites, clinical consultants, and key opinion leaders to represent the interests of the company</li>
<li>Support corporate strategic and organizational initiatives</li>
<li>Assist with commercial activities as needed</li>
<li>Complete assigned tasks thoroughly, accurately, and on time</li>
<li>Adhere to rigorous ethical standards </li>
<li>Travel up to 20% domestically and internationally for scientific meetings</li>
</ul>
Requirements
<ul>
<li>Advanced degree e.g. Ph.D., Pharm.D., MS, or equivalent</li>
</ul>
<ul>
<li>Strong track record of scientific and clinical inquiry</li>
<li>Understand statistical concepts and clinical trial design</li>
<li>Understand the connection between nonclinical data and clinical data</li>
<li>Possess excellent communication skills (both written and verbal)</li>
<li>Learn quickly, follow complex directions under pressure </li>
<li>Multi-task while remaining organized and attentive to detail</li>
<li>Work hard, be a trustworthy and collaborative team player</li>
<li>Take initiative and solve problems of moderate complexity</li>
<li>Demonstrate sound judgement in terms of handling complex, confidential, and regulated information</li>
<li>Lead both directly and by example</li>
</ul>
<ul>
<li>Preferred, but not required:</li>
<ul>
<li>At least 4 years of experience with clinical trial design and execution</li>
<li>At least 4 years of pharmaceutical industry experience </li>
<li>Experience with regulatory submissions and interactions</li>
</ul>
</ul>
Estimated compensation 170-190K/year USD DOE
Benefits
<ul>
<li>401(k) plan with company match </li>
<li>Medical, dental, and vision plans </li>
<li>Company-offered Life and Accidental Death &amp; Dismemberment (AD&amp;D) insurance </li>
<li>Company-provided short and long-term disability benefits </li>
<li>Unique offerings of Pet Insurance and Legal Insurance</li>
<li>Employee Assistance Program</li>
<li>Employee Discounts</li>
<li>Professional Development</li>
<li>Health Saving Account (HSA)</li>
<li>Flexible Spending Accounts</li>
<li>Various incentive compensation plans</li>
<li>Accident, Critical Illness, and Hospital Indemnity Insurance </li>
<li>Mental Health resources </li>
<li>Paid leave benefits for new parents </li>
</ul>
A note to recruiters:
We do not allow external search party solicitation. Presentation of candidates without written permission from the Ascendis Pharma Inc. Human Resources team (specifically from: Talent Acquisition Partner or Human Resources Director) is not allowed. If this occurs your ownership of these candidates will not be acknowledged.

Senior Clinical Scientist - Job ID: SCS

<h3>Job Description</h3>
Job Description Principal Formulation Chemist Duke Cannon Supply Co. is a growth-oriented CPG company that operates with an entrepreneurial mindset – and has become one of the fastest-growing brands in the men’s grooming category. Our mission is to better the day of hard-working men, and we fulfill this mission through both the products we build and the conversations we create. We have ambitions to become a household brand by taking share from large national players while having fun and giving back to veterans (our cause). We’re looking to hire smart, fun, and wildly talented folks to join us on our journey. We are currently seeking applicants for the role of Principal Formulation Chemist. This position will be responsible for all lab operations, new formula creation and associated testing, line extensions, formula and new ingredient research, documentation, and commercialization with internal and external partners.&nbsp; This role will lead products from ideation through launch and beyond, with heavy involvement in formulation, research, and scale-up activities.&nbsp; Successful candidates will have a proven track record of in-market formulations, formulation technical acumen across multiple product forms (surfactant experience required), the ability to work independently, plan strategically, pivot quickly, and build strong partnerships.&nbsp; PRIMARY RESPONSIBILITIES:
<ul>
<li>Formulation &amp; Development:&nbsp;Formulate in-house fragrance line extensions, innovation projects, reformulations, second source ingredient qualifications (cost-op), and assist in smooth technology transfers to meet critical deadlines, cost targets, and established product aesthetics/performance parameters.&nbsp; Partner closely with TPMs to ensure seamless launches.</li>
<li>Research &amp; Innovation Pipeline: Drive brand growth through regular research and evaluation of new product and ingredient technologies within the competitive, raw material, and technological landscape.&nbsp; Attend conferences, seminars, etc., as opportunities arise.&nbsp; Leverage available resources (analytics, internal SMEs, consumer panels, etc.) to deepen Duke Cannon’s understanding of competitive landscape and innovate our BIGGEST bets yet. </li>
<li>Product Evaluation: Evaluate formulas through various sensory or consumer testing methods to determine aesthetic and performance fitness versus established product pillars and benchmarks.&nbsp; </li>
<li>Testing &amp; Scale-Up:&nbsp;Coordinate and execute product testing, ensuring products meet minimum testing requirements (PET, stability, HRIPT, heavy metals &amp; 1, 4-Dioxane levels, etc.).&nbsp; Facilitate smooth transition of products from lab to production scale with manufacturing partners.&nbsp; Attend pilot and first production batches at TPMs to ensure they are executed with excellence and positioned to sustain brand growth.&nbsp; </li>
<li>Laboratory Operations: Responsible for lab equipment maintenance and calibration, ingredient management, lab SOP management, workflow, and daily lab functionality.</li>
<li>Document Management:&nbsp;Ensure product documentation is accurate and complete in advance of each launch.&nbsp; Partner with Quality/Regulatory to ensure all requirements and deadlines (eg: WERCS listing) are met.</li>
</ul>
 QUALIFICATIONS:
<ul>
<li>Bachelor’s degree in chemistry, biology, engineering, or related field. </li>
<li>10+ years of experience in a dynamic CPG formulation role, specifically in the personal care industry.</li>
<li>Experience formulating across multiple product forms, including surfactants (deep surfactant knowledge a MUST), emulsions, hot pours, hydroalcoholics, OTCs.&nbsp; Color matching experience preferred, but not essential.</li>
<li>Technical expertise to solve complex formulation issues.</li>
<li>Proven experience commercializing multiple consumer product goods.</li>
<li>Collaborative communication and interpersonal skills.</li>
<li>Creative thinker with a strategic approach to decision-making.</li>
<li>Ability to manage multiple projects simultaneously and meet tight deadlines.</li>
<li>Experience with controlled document systems.</li>
</ul>
 COMPANY CULTURE Duke Cannon Supply Co. offers a fast-paced environment where decisions are vetted quickly, and opportunities are relentlessly pursued.&nbsp; We work hard, but we value flexibility as well.&nbsp; We have an informal culture with an emphasis on having fun (we sell soap, after all), though we have the most fun when we exceed our goals. The company’s leaders are dedicated to the growth and development of the team; as such, we want to ensure that our people have a rich and rewarding experience with unique opportunities to grow.&nbsp; Duke Cannon Supply Co.’s Main Lodge (aka the office) is in Minneapolis’ North Loop, one of the city’s most vibrant and walkable neighborhoods, with award-winning restaurants, fashionable boutiques, live music and Major League Baseball just steps away. SALARY AND BENEFITS Duke Cannon offers a competitive market salary and bonus based on role and professional experience. The salary range for this role is $100,000 - $125,000. Our benefits are top-notch and include health &amp; dental insurance, HSA and 401k programs supported by regular company contributions, a tuition reimbursement program, and monthly parking stipend.&nbsp; We also host monthly moments of Team camaraderie ranging from community service events to social hours in the Main Lodge (aka the office) to Lunch &amp; Learns covering business, team, and industry topics. Duke Cannon provides equal access to and opportunity in employment without regard to race, color, creed, religion, national origin, gender, age, marital status, disability, public assistance status, veteran status, sexual orientation, gender identity, or gender expression. &nbsp;
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zijdZbISFq

Principal Formulation Chemist

<h3>Job Description</h3>
Job DescriptionEfficient Foundation Models for Edge Intelligence
We are seeking passionate and skilled interns to join our cutting-edge research team at Mitsubishi Electric Research Laboratories (MERL), focusing on efficient and sustainable AI. This internship offers a unique opportunity to contribute to next-generation machine learning techniques that enable real-time, edge, and energy-efficient AI systems — with the ultimate goal of publishing at top-tier AI venues.
Research Focus Areas
<ul>
<li>Edge AI, real-time AI, and compact neural architectures</li>
<li>Energy-efficient and hardware-friendly AI</li>
<li>On-device, on-premise, and embedded-system AI</li>
<li>Generative and multi-modal foundation models with resource constraints</li>
</ul>
Qualifications
<ul>
<li>Advanced research experience in generative models, efficient architectures, or foundation models (LLM, VLM, LMM, FoMo)</li>
<li>Strong understanding of state-of-the-art machine learning and optimization techniques</li>
<li>Proficiency in Python and PyTorch, with familiarity in other deep learning frameworks</li>
<li>Proven research record and motivation for publication in leading AI conferences</li>
</ul>
Internship Details
<ul>
<li>Duration: Approximately 3 months</li>
<li>Start Date: Flexible</li>
<li>Objective: Conduct high-quality research leading to publications in premier AI conferences</li>
</ul>
If you are a highly motivated researcher eager to push the boundaries of efficient and sustainable AI, we encourage you to apply. Join us in shaping the future of intelligent systems that are not only powerful but also responsible and sustainable.
The pay range for this internship position will be 6-8K per month.
Mitsubishi Electric Research Labs, Inc. "MERL" provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, disability or genetics. In addition to federal law requirements, MERL complies with applicable state and local laws governing nondiscrimination in employment in every location in which the company has facilities. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.
MERL expressly prohibits any form of workplace harassment based on race, color, religion, gender, sexual orientation, gender identity or expression, national origin, age, genetic information, disability, or veteran status. Improper interference with the ability of MERL’s employees to perform their job duties may result in discipline up to and including discharge.
Working at MERL requires full authorization to work in the U.S and access to technology, software and other information that is subject to governmental access control restrictions, due to export controls. Employment is conditioned on continued full authorization to work in the U.S and the availability of government authorization for the release of these items, which might include without limitation, obtaining an export license or other documentation. MERL may delay commencement of employment, rescind an offer of employment, terminate employment, and/or modify job responsibilities, compensation, benefits, and/or access to MERL facilities and information systems, as MERL deems appropriate, to ensure practical compliance with applicable employment law and government access control restrictions. 
In addition to base pay, interns receive a relocation stipend, covered travel to and from MERL, and a monthly Charlie Card for local commuting. Interns are invited to participate in weekly social gatherings and professional development opportunities, including research talks by both internal and external speakers. Interns who meet the 90-day waiting period are also eligible for health insurance coverage. MERL provides immigration support for qualified candidates as needed. Employment is considered “at-will,” and the Company reserves the right to modify base salary or any other compensation program at any time, including for reasons related to individual performance, departmental or Company performance, and market conditions.

Internship - Efficient Foundation Models for Edge Intelligence

<h3>Job Description</h3>
Job DescriptionCompany Description 
About Chamberlain University Chamberlain University has a 130-year history and the mission to educate, empower, and embolden diverse healthcare professionals who advance the health of people, families, communities, and nations. Our regionally accredited University is comprised of the College of Nursing and the College of Health Professions. Our College of Nursing offers a Bachelor of Science in Nursing (BSN) degree program at 23 locations and online post-licensure degree programs and certificates including RN to BSN, RN to MSN, a Master of Science in Nursing (MSN) with six Specialty Tracks, and a Doctor of Nursing Practice (DNP). Our College of Health Professions offers online options with a Master of Public Health degree, Master of Physician Assistant Studies, Public Health Certificate programs, and a Master of Social Work degree. Learn more about Chamberlain University, part of Adtalem Global Education, at <a href="http://www.chamberlain.edu" target="_blank">www.chamberlain.edu</a>. There is one very significant way Chamberlain is different than other Universities - Chamberlain Care®. Healthcare education is offered in a culture of service excellence and care in four ways: care for self, care for colleagues, care for patients/clients, care for all. By living Chamberlain Care®, we’ve built a culture in which colleagues and students thrive and we graduate extraordinary healthcare professionals who transform the health of people worldwide. Chamberlain Care® is the guiding principle we provide to each other and to our students to help our students achieve their goals, reach their dreams and impact healthcare at a national level. If you're ready to live Chamberlain Care®, we invite you to apply today!
Job Description 
Opportunity at a Glance
We are interested in developing long-term relationships with superior instructors who have high professional standards, excellent communication skills, enthusiasm and a commitment to providing the finest practitioner-focused education.
We are seeking primarily Industry Professionals to share their knowledge and experience with undergraduate BSN nursing students on-site in&nbsp;St. Louis, MO.
Responsibilities
<ul>
<li>Develops and provides students with an approved Adtalem Global Education syllabus that follows a template established by the local campus, and which includes the terminal course objectives.</li>
</ul>
<ul>
<li>Organizes, prepares, and regularly revises and update all course materials.</li>
</ul>
<ul>
<li>Uses appropriate technological options for online technologies and course-related software, including Websites, e-mail, and online discussions for preparing the course and making it accessible to students.</li>
</ul>
<ul>
<li>Models effective oral and written communications that engage the students, provide clarity, and improve student learning.</li>
</ul>
<ul>
<li>Sets clear expectations for the course by publishing course terminal objectives, assignment/examinations dates, and weight the distribution of various evaluation categories.</li>
</ul>
<ul>
<li>Ensures that the content and level of material included on exams correspond to the course terminal objectives.</li>
</ul>
<ul>
<li>Demonstrates consistency and fairness in the preparation and grading of exams, and provide timely feedback to students.</li>
</ul>
<ul>
<li>Completes other duties as assigned.</li>
</ul>
<ul>
<li>Performs other duties as assigned</li>
</ul>
<ul>
<li>Complies with all policies and standards</li>
</ul>
Qualifications 
<ul>
<li>Master's Degree is required for all faculty positions (with 18 graduate hours in the subject being taught for undergraduate teaching). Required</li>
<li>Faculty must have requisite subject matter expertise and outstanding communication skills.</li>
<li>Faculty must also have excellent motivational and instructional skills in a diverse and non-traditional environment.</li>
<li>Must be able to work in a collegial manner and facilitate the efforts of diverse groups.</li>
<li>Additional requirements driven by state licensing or accreditation considerations may apply. Required</li>
</ul>
 Additional Information 
Chamberlain Visiting Professor Position - Campus: In support of the pay transparency laws enacted across the country, the expected compensation rate for this position is between $1,120 per assignment to $7,245 per assignment, depending on the candidate’s education and experience. Actual pay may be adjusted based on job-related factors permitted by law, such as type of course taught; experience and training; geographic location; licensure and certifications; market factors; departmental budgets; and responsibility. Our Talent Acquisition Team will be happy to answer any questions you may have, and we look forward to learning more about your salary requirements.
Equal Opportunity – Minority / Female / Disability / V / Gender Identity / Sexual Orientation

Microbiology Faculty (part-time)

<h3>Job Description</h3>
Job Description
Job Title: Chemist II Location: &nbsp;Monroeville, PA 15146 Duration: 06-month contract on W2 + possible extension or conversion Shift: Mon-Fri 8:00am-5:00pm Schedule: Schedule is flexible after the training period with start times between 6:00am-8:00am, working 8 hours/day.
Pay rate - $25/hr on w2(without Benefits)
JOB DESCRIPTION: Summary: The Chemist II will be a part of the Monroeville Business and Technology Center Photochromics team and involved in the execution of experiments related to product formulation and testing. The goal of this team is to develop new products through fundamental understanding of formulation and application. Specifically, you will work closely with formulators, chemists, and scientists to assist in the growth and development of Transitions products.
Key Responsibilities: • Following standard operating procedures and industry standards for formula mixing, sample preparation, and testing • Precise measurement and mixing of formula ingredients described by a formulation log • Preparing test specimens for a variety of tests • Creating a collaborative and inclusive work environment • Upholding safety standards for the team, including wearing appropriate personal protective equipment and following safety guidelines • Documenting and reporting experimental details • Keen observation of experimental details and external factors • Time management and work efficiency • Independently planning and executing all aspects of an experiment following a discussion of objectives with the supervisor • Interpreting data and making recommendations for future work
Qualifications: • Bachelor’s Degree in a scientific or technical field • 0-1 years of laboratory experience • Experience with coatings formulation is desired • Strong attention to detail and ability to keep track of multiple project tasks
PPE: Any PPE required will be supplied by the client

Chemist

<h3>Job Description</h3>
Job Description
BluePath Labs is a fast growing research and management consulting company focused on the challenging research problems for both government and private sector clients. BluePath is looking for one (1) Defense Research Analyst Intern to support open-source research in the defense and military aerospace sectors. Candidates must be a U.S. citizen to apply. These internships are year-around with possible full-time employment after one's graduation. There are no end-dates for the internship. 
TheDefense Research Analyst Intern must be able to read and translate source documents and publications in Mandarin. There is no specific undergraduate or graduate degree major requirement but there is a preference for candidates with previous technical analysis of the Chinese aerospace and defense sectors.
TheDefense Research Analyst Intern will report to a BluePath Research Analyst and work as a part of a team on data collection, developing a keyword searchable database and reference system, and supporting research analysis. The primary work location will be at BluePath offices near Foggy Bottom at 2101 L ST NW. Washington, D.C. This position is currently remote work until further notice.
Primary responsibilities include but are not limited to:
<ul>
<li>Data collection, scanning, and entry. </li>
<li>Open-source research and analysis</li>
</ul>
Required Qualifications:
<ul>
<li>U.S. citizen</li>
<li>Junior/Senior undergraduate, currently in a Master's program, or recent graduate.</li>
<li>Strong Mandarin reading and translating skills. (ILR 2+ or HSK 5)</li>
<li>Commit to at least 15-25hrs/week and 5-6 months. </li>
<li>Intellectually curious with strong attention to detail.</li>
<li>Personal initiative and drive.</li>
<li>Able to work independently with minimal oversight while meeting weekly goals.</li>
<li>Familiarity with Microsoft Excel and other database products.</li>
</ul>
Preferred Qualifications
<ul>
<li>Able to be an intern until May 2023.</li>
<li>ILR 3+ for Reading/Writing or HSK 6.</li>
<li>Previous research and data collection with Mandarin publications.</li>
<li>Previous research and technical analysis of Chinese aerospace and defense sectors.</li>
<li>Coding language such as python. </li>
<li>Interest in data science and data visualizations.</li>
</ul>
Job Type: Internship
Salary: $15.00-$25.00 /hour depending on experience.
About BluePath
BluePath Labs combines mission and business insights with advanced technologies to deliver measurable performance improvements for our clients. BluePath is dedicated to surpassing client expectations by always living by our core values of integrity, professionalism, and resilience.BluePath's extensive experience in Government, Military, Commercial, and Academic environments is unique among small businesses and a core differentiator of our solutions. Our multidisciplinary background allows us to solve diverse and complex problems. Most importantly, we work closely with our clients to frame problems correctly, optimize processes, leverage technologies, and implement enduring solutions. Labs are where ideas are born, experiments occur, and breakthroughs happen. It is the hallmark of BluePath's culture.
<a href="https://www.bluepathlabs.com/" target="_blank">https://www.bluepathlabs.com/</a>
BluePath is an Equal Opportunity Employer.

China Defense Research Analyst Internship

<h3>Job Description</h3>
Job Description
Job description:
<ul>
<li>
We are currently seeking a highly motivated and passionate scientist to join our team in Immunology Discovery based in Cambridge MA.
</li>
<li>
In this role, the candidate will collaborate with multiple cross-functional teams to advance portfolio projects, with a particular emphasis on supporting in vitro data generation. 
</li>
<li>
Responsibilities include performing and adapting cell-based in vitro protocols in a timely manner across diverse cell systems, data analysis and effective communication of results, and collaboration across multiple teams. 
</li>
<li>
The position offers a unique opportunity for a talented scientist to work in a dynamic, innovative, and multi-disciplinary environment to develop their career at the interface of basic research and early drug discovery. 
</li>
<li>
The position requires ability to work independently, demonstrate excellent technical, written and oral communication skills and work very well in a collaborative team environment.
</li>
<li>
Human colon organoid culture, passaging, and plating for experiments to support the group
</li>
<li>
Perform cell-based assays using cell lines and mammalian primary cells
</li>
<li>
Test biologic and small molecules in cell-based assays for functional readouts including cell proliferation, cytokine release, and gene expression.
</li>
<li>
Perform advanced molecular and cellular biology techniques (including but not limited to FACS, ELISA, MSD, HTRF, qPCR)
</li>
<li>
Responsibilities may include processing animal tissue ex vivo and isolation of immune cells from human and animal tissue or blood
</li>
<li>
Work independently on the design, execution and interpretation of experimental results to validate hypotheses related to the project need
</li>
<li>
Maintain close communication with multiple groups to support human colon organoid cell needs
</li>
<li>
Implement and innovate new experimental protocols/techniques as needed
</li>
<li>
Analyze, interpret, document and report data consistently, concisely and rigorously, both to individual stakeholders and in group settings
</li>
<li>
Demonstrate scientific excellence through dedication to multiple projects in a fast-paced multi-disciplinary environment
</li>
<li>
Impact projects mostly through lab-based activities
</li>
</ul>
Qualifications 
<ul>
<li>
Must have a bachelor's degree in Biological Science or related field with 2+ years of experience in biotech or pharma setting (industry experience)
</li>
<li>
Experience in in vitro cell culture (sterile techniques, handling challenging cell types) is required.
</li>
<li>
Experience with primary epithelial cells and human colon organoids is required.
</li>
<li>
Experience with immune cells including myeloid cells (monocytes macrophages or dendritic cells) is required.
</li>
<li>
Experience in immunoassays including multi-color flow cytometry and ELISA (or MSD, HTRF) is required.
</li>
<li>
Experience with gene expression analysis by qPCR is required
</li>
<li>
Experience with ex vivo animal tissue processing is a plus.
</li>
<li>
Ability to learn new skills and apply them in a fast-paced research environment.
</li>
<li>
Creativity, problem-solving, and attention to details.
</li>
<li>
Excellent oral and written communication and collaboration skills.
</li>
<li>
Ability to work independently as well as in a team.
</li>
<li>
Proven flexibility to deal with changing timelines and shifting work priorities.
</li>
<li>
Experience with in vitro assays with primary human immune cells (ie myeloid, PBMCs)
</li>
<li>
Experience with molecular and cellular analysis techniques including qPCR, MSD, ELISA, flow cytometry
</li>
<li>
Experience with cell-based assay development is a plus.
</li>
</ul>
Benefits:
Healthcare Insurance: Synectics offers eligible employees and their dependents healthcare coverage through BlueCross BlueShield of Illinois. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics. Premiums are subsidized by Synectics. 
Dental Insurance: Synectics offers eligible employees and their dependents a dental plan through MetLife. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics. 
Vision Insurance: Synectics offers eligible employees vision insurance through VSP. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics.401(k) Plan: The Synectics Inc. Investment Savings Retirement Plan. Synectics offers all employees who are 21 years of age or older the opportunity to invest in the 401(k) Plan on the first enrollment date that is at least 30 days after employment begins. Enrollment dates are each January 1st, April 1st, July 1st, and October 1st.
Technical Certification Bonus: Synectics is pleased to award its employees a bonus of up to $500 for an approved professional certification. In determining the bonus amount, Synectics will consider the cost of the test(s) for any certification relating to your current position, achieved during your employment with us. Only one Certification Bonus per calendar year may be awarded per employee. Only current, active employees will be eligible to receive this bonus. It will be awarded 90 days after the Synectics office has received documentation confirming the successful completion of the certification.
Synectics is an equal opportunity employer.

Biologist

<h3>Job Description</h3>
Job Description
We are seeking an experienced and motivated Geotechnical Department Manager to lead our growing team in Auburn Hills, Michigan. This position is responsible for managing a variety of geotechnical projects across industrial, commercial, and residential markets. The ideal candidate will bring strong technical expertise, proven leadership skills, and a passion for developing teams and building client relationships.
As the Geotechnical Department Manager, you will oversee department operations, ensure quality project delivery, manage budgets, and play a key role in business development and strategic growth.
Key Responsibilities
Leadership and Department Management
<ul>
<li>Lead and mentor a team of geotechnical engineers and field staff, fostering a positive and productive work environment.</li>
<li>Oversee daily department operations, project schedules, and quality control processes.</li>
<li>Manage staffing, workload distribution, and performance evaluations.</li>
</ul>
Strategic Planning and Financial Oversight
<ul>
<li>Develop long-term goals and business plans to support company growth.</li>
<li>Manage departmental budgets, project profitability, and resource allocation.</li>
<li>Review and approve departmental expenses, invoices, and client billing.</li>
</ul>
Project Management
<ul>
<li>Oversee all phases of geotechnical and construction materials testing projects.</li>
<li>Collaborate with architects, civil engineers, and other technical teams to ensure successful project completion.</li>
<li>Maintain client satisfaction by delivering high-quality work on schedule and within budget.</li>
</ul>
Business Development and Client Relations
<ul>
<li>Build and maintain relationships with clients and industry partners.</li>
<li>Support proposal development, pricing strategies, and project bids.</li>
<li>Represent the company at industry events and networking opportunities.</li>
</ul>
Policy, Compliance, and Quality Assurance
<ul>
<li>Develop and enforce department policies, procedures, and quality standards.</li>
<li>Ensure compliance with all local, state, and federal regulations.</li>
<li>Promote continuous improvement and best practices within the department.</li>
</ul>
Qualifications
<ul>
<li>Bachelor's Degree in Civil Engineering or a related field.</li>
<li>Licensed Professional Engineer (P.E.) in Michigan, or the ability to obtain licensure.</li>
<li>Minimum of 10 years of geotechnical or civil engineering experience with increasing responsibility.</li>
<li>Proven experience managing teams, budgets, and multi-disciplinary projects.</li>
<li>Strong working knowledge of geotechnical design software and Microsoft Office applications.</li>
<li>Familiarity with Michigan codes, regulations, and site development standards.</li>
</ul>
Preferred Skills and Attributes
<ul>
<li>Demonstrated success in business development and client relationship management.</li>
<li>Strong analytical and problem-solving abilities.</li>
<li>Excellent communication, leadership, and mentoring skills.</li>
<li>Experience managing profitability, budgets, and collections.</li>
<li>Self-motivated with a proactive approach to achieving goals.</li>
</ul>
Work Environment and Physical Requirements
<ul>
<li>Primarily office-based role with some field visits to project sites.</li>
<li>Must be able to lift up to 25 pounds occasionally and perform site inspections as needed.</li>
<li>Requires the use of standard office and field equipment.</li>
</ul>
Schedule and Travel
<ul>
<li>Full-time position, Monday through Friday, 8 a.m. to 5 p.m.</li>
<li>Occasional overtime may be required.</li>
<li>Local travel to project sites is expected.</li>
</ul>
Compensation and Benefits
<ul>
<li>Salary range: $120,000 to $150,000 per year plus bonus opportunities up to 15 percent.</li>
<li>Comprehensive benefits package including medical, dental, and vision insurance.</li>
<li>401 (k) with profit sharing, short-term and long-term disability, and life insurance.</li>
<li>Paid time off, maternity and paternity leave, volunteer time off, tuition assistance, and fitness reimbursement.</li>
<li>Health insurance coverage begins on the first of the month following 30 days of employment.</li>
<li>Hybrid work schedule with 2 to 3 days in the office per week.</li>
<li>Relocation assistance and potential sign-on bonus available.</li>
</ul>

Senior Geotechnical Engineer

<h3>Job Description</h3>
Job DescriptionSr. R&amp;D Formulation Scientist – Biologics ????&nbsp;El Segundo, CA (Onsite) ????&nbsp;Direct Hire | Biopharmaceuticals ????&nbsp;$150,000 – $160,000/year (based on experience) About the Role: Yoh is seeking a&nbsp;Sr.&nbsp;R&amp;D Formulation Scientist – Biologics&nbsp;to join our client’s innovative team in El Segundo, CA. This is a unique opportunity to lead formulation development efforts for biologic therapeutics in a cutting-edge biopharmaceutical environment. The ideal candidate is a creative and driven scientist with deep expertise in biologics, drug product formulation, and protein formulation (mAbs). Key Responsibilities: 
<ul>
<li>Design and develop formulations for biologic drug products.</li>
<li>Expertise in biologics, drug product formulation, and protein formulation (mAbs).</li>
<li>Conduct hands-on laboratory experiments and coordinate with external testing partners.</li>
<li>Collaborate cross-functionally with product development, process engineering, analytical development, and other engineering teams to advance drug development programs.</li>
</ul>
Qualifications: 
<ul>
<li>PhD in Pharmaceutics, Biochemical Engineering, Chemical Engineering, Organic Chemistry, or a related field.</li>
<li>Minimum of 5 years of industry experience in biologics production and protein&nbsp;formulation i.e. mAbs.</li>
<li>Proven experience with regulatory submissions and addressing regulatory inquiries.</li>
<li>Demonstrated success in biologics and protein formulation and development, supported by peer-reviewed publications and/or scientific presentations.</li>
<li>Strong knowledge of biologic and protein formulation development across various dosage forms, including characterization and scale-up.</li>
<li>Deep understanding of protein stability and product quality attributes.</li>
</ul>
#IND-SPG Estimated Min Rate: $150000.00 Estimated Max Rate: $160000.00 What’s In It for You? We welcome you to be a part of the largest and legendary global staffing companies to meet your career aspirations. Yoh’s network of client companies has been employing professionals like you for over 65 years in the U.S., UK and Canada. Join Yoh’s extensive talent community that will provide you with access to Yoh’s vast network of opportunities and gain access to this exclusive opportunity available to you. Benefit eligibility is in accordance with applicable laws and client requirements. Benefits include: 
<ul>
<li>Medical, Prescription, Dental &amp; Vision Benefits (for employees working 20+ hours per week)</li>
<li>Health Savings Account (HSA) (for employees working 20+ hours per week)</li>
<li>Life &amp; Disability Insurance (for employees working 20+ hours per week)</li>
<li>MetLife Voluntary Benefits</li>
<li>Employee Assistance Program (EAP)</li>
<li>401K Retirement Savings Plan</li>
<li>Direct Deposit &amp; weekly epayroll</li>
<li>Referral Bonus Programs</li>
<li>Certification and training opportunities</li>
</ul>
 Note: Any pay ranges displayed are estimations. Actual pay is determined by an applicant's experience, technical expertise, and other qualifications as listed in the job description. All qualified applicants are welcome to apply. Yoh, a Day &amp; Zimmermann company, is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. Visit <a href="https://www.yoh.com/applicants-with-disabilities" target="_blank">https://www.yoh.com/applicants-with-disabilities</a> to contact us if you are an individual with a disability and require accommodation in the application process. For California applicants, qualified applicants with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act. All of the material job duties described in this posting are job duties for which a criminal history may have a direct, adverse, and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.Company DescriptionFounded in 1940, Yoh operates from 75 locations throughout North America and is headquartered in Philadelphia, PA. Yoh was the nation’s first technology staffing firm. As a business unit of Day &amp; Zimmermann, Yoh has a flourishing global footprint, as our parent company operates from more than 150 worldwide locations. Company Website: <a href="https://www.yoh.com/" target="_blank">https://www.yoh.com/</a> 
<h3>Company Description</h3>
Founded in 1940, Yoh operates from 75 locations throughout North America and is headquartered in Philadelphia, PA. Yoh was the nation’s first technology staffing firm. As a business unit of Day &amp; Zimmermann, Yoh has a flourishing global footprint, as our parent company operates from more than 150 worldwide locations.\r\nCompany Website: <a href="https://www.yoh.com/" target="_blank">https://www.yoh.com/</a>

Sr. R&D Formulation Scientist - Biologics

<h3>Job Description</h3>
Job Description
 
Chemical Operator – I
 We are looking to add a motivated &amp; compassionate chemical operator to our Tedia team to work out of our Fairfield, Ohio location. We are a customer-driven company that provides high-purity solvents for life science, biotechnology, pharmaceutical, laboratory, and industrial applications. We are in need of a strong contributor to help us stay focused on two of our core values and they are: Safety and Quality. 
This individual must possess a solid understanding of chemical processes and mechanics. You can expect to work as an integral part of the production team and may be responsible for retrieving, weighing and mixing chemical ingredients, monitoring equipment during the chemical process, record information and assist in the planning and improvement of processes or products by complying with all company, local, state, and federal safety and quality regulations. 
Tedia wants you to have everything you need to work in a safe, fun and productive environment so we are pleased to offer: 
<ul>
<li>Competitive compensation that allows for annual salary increases based on the environment and work performance along with generous vacation and sick time which includes 9 paid holidays and a matched 401(k) retirement plan! </li>
<li>Competitive health care benefits that include health, dental, vision, life insurance, along with a variety of voluntary benefits, i.e., short term &amp; long-term disability, critical illness and legal shield, etc. </li>
<li>Career growth and development i.e., education reimbursement, coaching, mentorships, and training programs. </li>
<li>Reward and recognition celebrations i.e., free monthly luncheons, monthly birthday celebrations, and service awards.</li>
</ul>
Core Responsibilities: 
<ul>
<li>Assure safety requirements are known and followed</li>
<li>Use proper PPE for assigned tasks</li>
<li>Notify supervisor immediately of any safety related issues</li>
<li>Set up and dismantle filling equipment</li>
<li>Blend chemicals for DNA blends</li>
<li>Process chemicals for Anhydrosolv solvents</li>
<li>Use instrumentation: GC (Assay), UV spectrophotometer (Optical Absorbance), and KF (water) to analyze in-process samples</li>
<li>Clean filling equipment, holding tanks, totes, reactors, and pumps according to procedure</li>
<li>Organize the production equipment in designated areas</li>
<li>Submit samples to the lab for analysis according to procedure</li>
<li>Be highly aware of quality issues and BOM</li>
<li>Fill drums, totes, bottles, and RC's according to BOM</li>
<li>Unload and charge tankers (bulk material) following the given instructions</li>
<li>Clean and pack columns with adsorbent material and activate the column</li>
<li>Steam waste adsorbent material for disposal</li>
<li>Assist Chemical Operators with charging reactors and with other requirements</li>
<li>Handle waste according to the established procedures</li>
<li>Complete the cleaning record form</li>
</ul>
Qualifications
<ul>
<li>Having knowledge and/or experience with chemistry and math knowledge is preferred</li>
<li>Independent thinking, strong organizational and planning abilities, and problem-solving skills are essential </li>
<li>Manufacturing experience</li>
</ul>
Education Requirements: 
<ul>
<li>High school diploma or G.E.D. required </li>
</ul>
Seniority Level: Entry level Chemical Operator I; non-exempt 
Employment Type: Full-time, 12 hour shifts-rotating schedule with rotating weekends. 
Industry: Chemical Manufacturing
Job Functions: Production/Chemical
Work Environment /Physical Demands: 
The physical requirements described are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform these essential functions. 
<ul>
<li>Able to wear respirator, safety shoes, goggles and/or safety glasses</li>
<li>Be comfortable working in a hazmat chemical environment</li>
<li>Able to stoop, bend, twist, and climb ladders and/or stairs</li>
<li>Use hands and arms to handle and reach </li>
<li>Able to walk, talk, and hear</li>
<li>Vision abilities: close vision, distance vision, and ability to adjust focus</li>
<li>Hand-eye coordination sufficient to place labels on bottles and boxes accurately</li>
<li>Able to move up to 70 lbs.</li>
<li>Able to lift up to 15 lbs. above shoulder height</li>
<li>Able to shift drums of product up to 300 lbs.</li>
<li>Able to work in hot and cold environment while wearing PPE.</li>
</ul>
 
 
 7PM to 7AM Rotating shift

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